Canonical Allele Identifier: CA393098485
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2151228618
gnomAD v4: 15-73367985-A-G
MyVariant Identifiers: chr15:g.73660326A>G (hg19) chr15:g.73367985A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367985A>G , CM000677.2:g.73367985A>G GRCh38
NC_000015.9:g.73660326A>G , CM000677.1:g.73660326A>G GRCh37
NC_000015.8:g.71447379A>G NCBI36
NG_009063.1:g.6280T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.286T>C MANE Select ENSP00000261917.3:p.Phe96Leu
ENST00000261917.3:c.286T>C ENSP00000261917.3:p.Phe96Leu
NM_005477.2:c.286T>C NP_005468.1:p.Phe96Leu
NM_005477.3:c.286T>C MANE Select NP_005468.1:p.Phe96Leu
Search 100 bp 5'
Search 100 bp 3'